1. Fortyfour probands with an additional 'marker' chromosome;Buckton, K.E.; Spowart, G.; Newton, M.S.; Evans, H.J.;Hum Genet,1985
2. Bisatellited extra small metacentric chromosome in newborns;Freidrich, V.; Nielsen, J.;Clin Genet,1974
3. Clinical and molecular analysis of five inv dup (15) patients;Robinson, W.P.; Binkert, F.; Gine, R.;Eur J Hum Genet,1993
4. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome;Ledbetter, D.H.; Riccardi, V.M.; Airhart, S.D.; Strobel, R.J.; Keenan, B.S.; Craw-ford, J.D.;N Engl J Med,1981
5. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome;Nicholls, R.D.; Knoll, J.H.M.; Butler, M.G.; Karam, S.; Lalande, M.;Nature,1989